Merkel Cells Activate Sensory Neural Pathways through Adrenergic Synapses

Neuron. 2018 Dec 19;100(6):1401-1413.e6. doi: 10.1016/j.neuron.2018.10.034. Epub 2018 Nov 8.

Abstract

Epithelial-neuronal signaling is essential for sensory encoding in touch, itch, and nociception; however, little is known about the release mechanisms and neurotransmitter receptors through which skin cells govern neuronal excitability. Merkel cells are mechanosensory epidermal cells that have long been proposed to activate neuronal afferents through chemical synaptic transmission. We employed a set of classical criteria for chemical neurotransmission as a framework to test this hypothesis. RNA sequencing of adult mouse Merkel cells demonstrated that they express presynaptic molecules and biosynthetic machinery for adrenergic transmission. Moreover, live-cell imaging directly demonstrated that Merkel cells mediate activity- and VMAT-dependent release of fluorescent catecholamine neurotransmitter analogs. Touch-evoked firing in Merkel-cell afferents was inhibited either by pre-synaptic silencing of SNARE-mediated vesicle release from Merkel cells or by neuronal deletion of β2-adrenergic receptors. Together, these results identify both pre- and postsynaptic mechanisms through which Merkel cells excite mechanosensory afferents to encode gentle touch. VIDEO ABSTRACT.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / physiology
  • Adrenergic Agents / metabolism*
  • Afferent Pathways / physiology*
  • Animals
  • Bacterial Capsules / metabolism
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Female
  • Ganglia, Spinal / cytology
  • Male
  • Merkel Cells / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Receptors, Adrenergic, beta-2
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Receptors, Serotonin, 5-HT3 / genetics
  • Receptors, Serotonin, 5-HT3 / metabolism
  • Skin / cytology
  • Skin / innervation
  • Synapses / physiology*
  • Synaptic Transmission / physiology*
  • Tyrosine 3-Monooxygenase / genetics
  • Tyrosine 3-Monooxygenase / metabolism
  • Vesicular Monoamine Transport Proteins / genetics
  • Vesicular Monoamine Transport Proteins / metabolism
  • Wnt1 Protein / genetics
  • Wnt1 Protein / metabolism

Substances

  • ADRB2 protein, mouse
  • Adrenergic Agents
  • Atoh1 protein, mouse
  • Basic Helix-Loop-Helix Transcription Factors
  • Receptors, Adrenergic, beta-2
  • Receptors, G-Protein-Coupled
  • Receptors, Serotonin, 5-HT3
  • Slc18a1 protein, mouse
  • Vesicular Monoamine Transport Proteins
  • Wnt1 Protein
  • capsular polysaccharide K14
  • Tyrosine 3-Monooxygenase